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Molecule
ID:102500
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₁₄N₅O₈P
Molecular Mass
363.220621
Exact Mass
363.05799906
Charge
0
InChI
InChI=1S/C10H14N5O8P/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(23-9)1-22-24(19,20)21/h2-3,5-6,9,16-17H,1H2,(H2,19,20,21)(H3,11,13,14,18)
InChIKey
RQFCJASXJCIDSX-UHFFFAOYSA-N
Canonic Smiles
OC1C(O)C(OC1n1cnc2c1nc(N)[nH]c2=O)COP(=O)(O)O
Isomeric Smiles
Nc1nc2c(ncn2C2OC(COP(=O)(O)O)C(O)C2O)c(=O)[nH]1
Calculated Properties
JChem
Acid pKa
1.0546672
H Acceptors
10
H Donor
6
LogD (pH = 5.5)
-5.2467523
LogD (pH = 7.4)
-6.360609
Log P
-2.9361746
Molar Refractivity
75.493996
Polarizability
28.927122
Polar Surface Area
201.75
Rotatable Bonds
4
Lipinski's Rule of Five
false
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Related Proteins
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General Information
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IUPAC name
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PubChem SID
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PubChem CID
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MP Biomedicals
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Data Source
Commercial Catalog
MP Biomedicals
02101908
Academic Data
PubChem
761
Names and Identifiers
IUPAC name
{[5-(2-amino-6-oxo-6,9-dihydro-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid
Synonyms
GUANOSINE-5'-MONOPHOSPHATE FREE ACID
GMP
IUPAC Traditional name
guanosine-5'-monophosphate
Registration numbers
EC Number
201-598-8
CAS Number
85-32-5
PubChem SID
162090533
PubChem CID
761
Molecule Details
MP Biomedicals
02101908
Free Acid
White crystalline powder
Purity: 98-100%
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
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Physical Property
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Safety Information
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Product Information
Properties
Physical Property
Melting Point
91-93°C
Source
Safety Information
RTECS
MF9283000
Source
MSDS Link
Download link
Source
Storage Condition
2-8°C
Source
Product Information
98-100%
Source
Download link
Source
Purity
Certificate of Analysis